CHRNA7 c.195+32707C>T

Variant ID: 15-32355947-C-T

NM_000746.5(CHRNA7):c.195+32707C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Four new loci associations discovered by pathway-based and network analyses of the genome-wide variability profile of Hirschsprung's disease.

Orphanet Journal Of Rare Diseases
Fernández, Raquel Ma RM; Bleda, Marta M; Núñez-Torres, Rocío R; Medina, Ignacio I; Luzón-Toro, Berta B; García-Alonso, Luz L; Torroglosa, Ana A; Marbà, Martina M; Enguix-Riego, Ma Valle MV; Montaner, David D; Antiñolo, Guillermo G; Dopazo, Joaquín J; Borrego, Salud S
Publication Date: 2012-12-28

Variant appearance in text: rs2175886
PubMed Link: 23270508
Variant Present in the following documents:
  • Main text
  • 1750-1172-7-103.pdf
View BVdb publication page



Gender-stratified gene and gene-treatment interactions in smoking cessation.

The Pharmacogenomics Journal
Lee, W W; Bergen, A W AW; Swan, G E GE; Li, D D; Liu, J J; Thomas, P P; Tyndale, R F RF; Benowitz, N L NL; Lerman, C C; Conti, D V DV
Publication Date: 2012-12

Variant appearance in text: rs2175886
PubMed Link: 21808284
Variant Present in the following documents:
  • NIHMS305090-supplement-3.pdf
View BVdb publication page